|Publication number||US7608115 B2|
|Application number||US 10/556,044|
|Publication date||Oct 27, 2009|
|Filing date||Apr 30, 2004|
|Priority date||May 9, 2003|
|Also published as||EP1631241A1, EP1631241B1, US20070174974, US20100005600, WO2004098550A1|
|Publication number||10556044, 556044, PCT/2004/6058, PCT/EP/2004/006058, PCT/EP/2004/06058, PCT/EP/4/006058, PCT/EP/4/06058, PCT/EP2004/006058, PCT/EP2004/06058, PCT/EP2004006058, PCT/EP200406058, PCT/EP4/006058, PCT/EP4/06058, PCT/EP4006058, PCT/EP406058, US 7608115 B2, US 7608115B2, US-B2-7608115, US7608115 B2, US7608115B2|
|Inventors||Roland de la Mettrie|
|Original Assignee||L'oreal S.A.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (101), Non-Patent Citations (14), Referenced by (2), Classifications (32), Legal Events (5)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application claims the right to priority based on French Application No. 0305636, filed May 9, 2003, and claims the benefit of U.S. Provisional Application No. 60/513,577, filed Oct. 24, 2003, the content of both of which is incorporated herein by reference in its entirety.
The present invention relates to a novel process for treating keratin fibres by applying heat. Such a process allows more pronounced results to be obtained.
It is known practice to dye keratin fibres, and in particular human hair, with dye compositions containing oxidation dye precursors, which are generally known as oxidation bases, such as ortho- or para-phenylenediamines, ortho- or para-aminophenols and heterocyclic compounds. These oxidation bases are colourless or weakly coloured compounds, which, when combined with oxidizing products, may give rise to coloured compounds by a process of oxidative condensation.
It is also known that the shades obtained with these oxidation bases may be varied by combining them with couplers or coloration modifiers, the latter being chosen especially from aromatic meta-diamines, meta-aminophenols, meta-diphenols and certain heterocyclic compounds such as indole compounds.
The variety of molecules used as oxidation bases and couplers allows a wide range of colours to be obtained.
It is also known practice to dye keratin fibres by direct dyeing. The process conventionally used in direct dyeing consists in applying to the keratin fibres direct dyes, which are coloured molecules and dyes that have an affinity for the fibres, in leaving these agents to act and then in optionally rinsing the fibres. The direct dyes may be chosen especially from dyes of the nitrobenzene, anthraquinone, nitropyridine, azo, xanthine, acridine or azine type, or methine dyes. These direct dyes may be of nonionic, anionic or cationic nature.
The colorations resulting therefrom are particularly chromatic but are, however, temporary or semi-permanent since the nature of the interactions which bind the direct dyes to the keratin fibre, and their desorption from the surface and/or from the core of the fibre, are responsible for their poor dyeing power, their lack of chromaticity and their poor wash-fastness or perspiration-fastness.
It is also known practice to use oxidizing agents to treat the hair, in particular in the case of the oxidation dyeing described above and in the case of permanently reshaping, bleaching or stripping the hair.
In the case of permanently reshaping (permanent-waving or relaxing) the hair, the oxidizing agent is used in fixing compositions that allow the hair to be fixed in the desired shape once the disulphide bonds of the hair have been broken using a reducing compound.
In the case of bleaching or stripping, the oxidizing agent is used to destroy the dyes present in the hair, whether they are melanin pigments in the case of bleaching naturally pigmented hair, or synthetic dyes in the case of dyed hair.
In any case, there is a need to increase the efficacy of the process concerned without increasing the concentrations of oxidizing agents, so as not to harm the integrity of the hair.
Finally, it is known practice to use cationic agents to condition the hair, i.e. to improve its cosmetic properties and in particular the softness or the ease of disentangling. This is particularly important when the treatment applied to the hair induces a risk of impairing the hair, for example dyeing, permanent-reshaping or bleaching treatments, or when these treatments are applied to hair that is already sensitized.
There is in this case also a need to increase the efficacy of these cationic agents without increasing their concentration, since these products are often sparingly degradable and the amount thereof in wastewater should thus be limited.
One of the aims of the present invention is to provide a novel process for treating keratin fibres more quickly and more efficiently.
One of the particular aims of the invention is to provide a process for treating keratin fibres that can in particular produce more intense colorations quickly and simply.
This aim is achieved by the present invention, one subject of which is a process for treating keratin fibres that comprises the application to the keratin fibres of a hair composition comprising, in a medium that is suitable for dyeing fibres, at least one active agent chosen from direct dyes, oxidation bases, couplers and oxidizing agents, followed by a step of heating the fibres coated with the hair composition, using a heating iron whose temperature is greater than or equal to 60° C.
It is thus possible to obtain faster and longer-lasting treatments, for example treatments that show better resistance to water and shampoo.
According to one embodiment, the process is preferably a process for dyeing keratin fibres in which the hair composition comprises at least one active agent chosen from direct dyes, oxidation bases and couplers and at least one oxidizing agent.
Hair dyes such as direct dyes, oxidation bases and couplers may be compounds that are conventionally synthesized or extracted from plant or animal species, this extract being obtained from the whole organism or a part thereof, for example using the leaves or the roots. The active substances that may be extracted from plant species are, for example, hydroxylated quinones, indigoids, hydroxyflavones, the A and B santalins, isatin and its derivatives, and brasilin and its hydroxylated derivative. The plant species that may be used in the present invention are for example, henna, indigo plant, camomile, annatto and alkanet. The animal species that may be used are, for example, cochineals.
The oxidation bases are generally chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols and heterocyclic bases, and the addition salts thereof.
Among the para-phenylenediamines that may be mentioned, for example, are para-phenylenediamine, para-tolylenediamine, 2-chloro-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,5-dimethyl-para-phenylenediamine, N,N-dimethyl-para-phenylenediamine, N,N-diethyl-para-phenylenediamine, N,N-dipropyl-para-phenylenediamine, 4-amino-N,N-diethyl-3-methylaniline, N,N-bis(β-hydroxyethyl)-para-phenylenediamine, 4-N,N-bis-(β-hydroxyethyl)amino-2-methylaniline, 4-N,N-bis(β-hydroxyethyl)amino-2-chloroaniline, 2-β-hydroxyethyl-para-phenylenediamine, 2-fluoro-para-phenylenediamine, 2-isopropyl-para-phenylenediamine, N-(β-hydroxypropyl)-para-phenylenediamine, 2-hydroxymethyl-para-phenylene-diamine, N,N-dimethyl-3-methyl-para-phenylenediamine, N-ethyl-N-(β-hydroxyethyl)-para-phenylenediamine, N-(β,γ-dihydroxypropyl)-para-phenylenediamine, N-(4′-aminophenyl)-para-phenylenediamine, N-phenyl-para-phenylenediamine, 2-β-hydroxyethyloxy-para-phenylene-diamine, 2-β-acetylaminoethyloxy-para-phenylenediamine, N-(β-methoxyethyl)-para-phenylenediamine, 4-amino-phenylpyrrolidine, 2-thienyl-para-phenylenediamine, 2-β-hydroxyethylamino-5-aminotoluene and 3-hydroxy-1-(4′-aminophenyl)pyrrolidine, and the addition salts thereof with an acid.
Among the para-phenylenediamines mentioned above, para-phenylenediamine, para-tolylenediamine, 2-isopropyl-para-phenylenediamine, 2-β-hydroxyethyl-para-phenylenediamine, 2-β-hydroxyethyloxy-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, N,N-bis(β-hydroxyethyl)-para-phenylenediamine, 2-chloro-para-phenylenediamine and 2-β-acetylaminoethyloxy-para-phenylenediamine, and the addition salts thereof with an acid, are particularly preferred.
Among the bis(phenyl)alkylenediamines that may be mentioned, for example, are N,N′-bis(β-hydroxyethyl)-N,N′-bis(4′-aminophenyl)-1,3-diaminopropanol, N,N′-bis(β-hydroxyethyl)-N,N′-bis(4′-aminophenyl)ethylenediamine, N,N′-bis(4-aminophenyl)-tetramethylenediamine, N,N′-bis(β-hydroxyethyl)-N,N′-bis(4-aminophenyl)tetramethylenediamine, N,N′-bis(4-methylaminophenyl)tetramethylenediamine, N,N′-bis(ethyl)-N,N′-bis(4′-amino-3′-methylphenyl)ethylenediamine and 1,8-bis(2,5-diamino-phenoxy)-3,6-dioxaoctane, and the addition salts thereof with an acid.
Among the para-aminophenols that may be mentioned, for example, are para-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 4-amino-3-hydroxymethylphenol, 4-amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4-amino-2-methoxymethylphenol, 4-amino-2-aminomethylphenol, 4-amino-2-(β-hydroxyethylaminomethyl)phenol, and 4-amino-2-fluorophenol, 4-amino-2-chloro-phenol, 4-amino-2,6-dichlorophenol, 4-amino 6-[(5′-amino 2′-hydroxy 3′-methylphenyl)methyl]2-methylphenol and bis-(5-amino 2-hydroxyphenyl)methane and the addition salts thereof with an acid.
Among the ortho-aminophenols that may be mentioned, for example, are 2-aminophenol, 2-amino-5-methylphenol, 2-amino-6-methylphenol and 5-acetamido-2-aminophenol, and the addition salts thereof with an acid.
Among the heterocyclic bases that may be mentioned, for example, are pyridine derivatives, pyrimidine derivatives and pyrazole derivatives.
Among the pyridine derivatives that may be mentioned are the compounds described, for example, in patents GB 1 026 978 and GB 1 153 196, such as 2,5-diaminopyridine, 2-(4-methoxyphenyl)amino-3-aminopyridine, 2,3-diamino-6-methoxypyridine, 2-(β-methoxyethyl)amino-3-amino-6-methoxypyridine and 3,4-diaminopyridine, and the addition salts thereof with an acid.
Other pyridine oxidation bases that are useful in the present invention include the 3-amino-pyrazolo[1,5-a]pyridine oxidation bases or the addition salts thereof described, for example, in patent application FR 2 801 308; By way of example, mention may be made of pyrazolo[1,5-a]pyrid-3-ylamine; 2-acetylaminopyrazolo[1,5-a]pyrid-3-ylamine; 2-morpholin-4-ylpyrazolo[1,5-a]pyrid-3-ylamine; 3-aminopyrazolo[1,5-a]pyridine-2-carboxylic acid; 2-methoxypyrazolo[1,5-a]pyrid-3-ylamine; (3-amino-pyrazolo[1,5-a]pyrid-7-yl)methanol; 2-(-3-aminopyrazolo-[1,5-a]pyrid-5-yl)ethanol; 2-(3-aminopyrazolo[1,5-a]-pyrid-7-yl)ethanol; (3-aminopyrazolo[1,5-a]pyrid-2-yl)-methanol; 3,6-diaminopyrazolo[1,5-a]pyridine; 3,4-diaminopyrazolo[1,5-a]pyridine; pyrazolo[1,5-a]-pyridine-3,7-diamine; 7-morpholin-4-ylpyrazolo[1,5-a]pyrid-3-ylamine; pyrazolo[1,5-a]pyridine-3,5-diamine; 5-morpholin-4-ylpyrazolo[1,5-a]pyrid-3-ylamine; 2-[(3-aminopyrazolo[1,5-a]pyrid-5-yl)(2-hydroxyethyl)-amino]ethanol; 2-[(3-aminopyrazolo[1,5-a]pyrid-7-yl)-(2-hydroxyethyl)amino]ethanol; 3-aminopyrazolo[1,5-a]-pyrid-5-ol; 3-aminopyrazolo[1,5-a]pyrid-4-ol; 3-aminopyrazolo[1,5-a]pyrid-6-ol; 3-aminopyrazolo[1,5-a]pyrid-7-ol; and also the addition salts thereof with an acid or with a base.
Among the pyrimidine derivatives that can be mentioned are the compounds described, for example, in patents DE 2 359 399; JP 88-169 571; JP 05-63124; EP 0 770 375 or patent application WO 96/15765, such as 2,4,5,6-tetraaminopyrimidine, 4-hydroxy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 2,4-dihydroxy-5,6-diaminopyrimidine and 2,5,6-triaminopyrimidine, and pyrazolopyrimidine derivatives such as those mentioned in patent application FR-A-2 750 048 and among which mention may be made of pyrazolo [1,5-a]pyrimidine-3,7-diamine; 2,5-dimethylpyrazolo[1,5-a]pyrimidine-3,7-diamine; pyrazolo[1,5-a]pyrimidine-3,5-diamine; 2,7-dimethylpyrazolo[1,5-a]pyrimidine-3,5-diamine; 3-aminopyrazolo[1,5-a]pyrimidin-7-ol; 3-aminopyrazolo-[1,5-a]pyrimidin-5-ol; 2-(3-aminopyrazolo[1,5-a]pyrimidin-7-ylamino)ethanol, 2-(7-aminopyrazolo[1,5-a]pyrimidin-3-ylamino)ethanol, 2-[(3-aminopyrazolo[1,5-a]pyrimidin-7-yl)(2-hydroxyethyl)amino]ethanol, 2-[(7-aminopyrazolo[1,5-a]pyrimidin-3-yl)(2-hydroxyethyl)amino]ethanol, 5,6-dimethylpyrazolo[1,5-a]pyrimidine-3,7-diamine, 2,6-dimethylpyrazolo[1,5-a]-pyrimidine-3,7-diamine, 2,5,N7,N7-tetramethylpyrazolo-[1,5-a]pyrimidine-3,7-diamine and 3-amino-5-methyl-7-imidazolylpropylaminopyrazolo[1,5-a]pyrimidine, and the addition salts thereof with an acid and the tautomeric forms thereof, when a tautomeric equilibrium exists.
Among the pyrazole derivatives that may be mentioned are the compounds described in patents DE 3 843 892 and DE 4 133 957 and patent applications WO 94/08969, WO 94/08970, FR-A-2 733 749 and DE 195 43 988, such as 4,5-diamino-1-methylpyrazole, 4,5-diamino-1-(β-hydroxyethyl)pyrazole, 3,4-diamino-pyrazole, 4,5-diamino-1-(4′-chlorobenzyl)pyrazole, 4,5-diamino-1,3-dimethylpyrazole, 4,5-diamino-3-methyl-1-phenylpyrazole, 4,5-diamino-1-methyl-3-phenyl-pyrazole, 4-amino-1,3-dimethyl-5-hydrazinopyrazole, 1-benzyl-4,5-diamino-3-methylpyrazole, 4,5-diamino-3-tert-butyl-1-methylpyrazole, 4,5-diamino-1-tert-butyl-3-methylpyrazole, 4,5-diamino-1-(β-hydroxyethyl)-3-methylpyrazole, 4,5-diamino-1-ethyl-3-methylpyrazole, 4,5-diamino-1-ethyl-3-(4′-methoxyphenyl)pyrazole, 4,5-diamino-1-ethyl-3-hydroxymethylpyrazole, 4,5-diamino-3-hydroxymethyl-1-methylpyrazole, 4,5-diamino-3-hydroxymethyl-1-isopropylpyrazole, 4,5-diamino-3-methyl-1-isopropylpyrazole, 4-amino-5-(2′-aminoethyl)amino-1,3-dimethylpyrazole, 3,4,5-triaminopyrazole, 1-methyl-3,4,5-triaminopyrazole, 3,5-diamino-1-methyl-4-methylaminopyrazole and 3,5-diamino-4-(β-hydroxyethyl)amino-1-methylpyrazole, and the addition salts thereof with an acid.
The couplers that are useful in the context of the present invention are, for example, meta-phenylenediamine, meta-aminophenol, meta-diphenol, naphthalene-based and heterocyclic couplers, and the addition salts thereof.
Examples that may be mentioned include 2-methyl-5-aminophenol, 5-N-(β-hydroxyethyl)amino-2-methylphenol, 6-chloro-2-methyl-5-aminophenol, 3-aminophenol, 1,3-dihydroxybenzene, 1,3-dihydroxy-2-methylbenzene, 4-chloro-1,3-dihydroxybenzene, 2,4-diamino-1-(β-hydroxyethyloxy)benzene, 2-amino-4-(β-hyroxyethylamino)-1-methoxybenzene, 1,3-diamino-benzene, 1,3-bis(2,4-diaminophenoxy)propane, 3-ureido-aniline, 3-ureido-1-dimethylaminobenzene, sesamol, 1-β-hydroxyethylamino-3,4-methylenedioxybenzene, α-naphthol, 2-methyl-1-naphthol, 6-hydroxyindole, 4-hydroxyindole, 4-hydroxy-N-methylindole, 2-amino-3-hydroxypyridine, 6-hydroxybenzomorpholine, 3,5-diamino-2,6-dimethoxypyridine, 1-N-(β-hydroxyethyl)-amino-3,4-methylenedioxybenzene and 2,6-bis(β-hydroxy-ethylamino)toluene and the addition salts thereof with an acid.
In general, the addition salts of the oxidation bases and of the couplers that may be used in the context of the invention are chosen especially from the addition salts with an acid, such as the hydrochlorides, hydrobromides, sulphates, citrates, succinates, tartrates, lactates, tosylates, benzenesulphonates, phosphates and acetates, and the addition salts with a base, such as sodium hydroxide, potassium hydroxide, ammonia, amines or alkanolamines.
The direct dyes that may be used according to the invention are preferably chosen from neutral, acidic or cationic nitrobenzene direct dyes, neutral, acidic or cationic azo direct dyes, neutral, acidic or cationic quinone and in particular anthraquinone direct dyes, azine direct dyes, triarylmethane direct dyes, indoamine direct dyes and natural direct dyes.
Among the benzenic direct dyes that may be used according to the invention, mention may be made, in a non-limiting manner, of the following compounds:
Among the azo direct dyes, mention may be made of the cationic azo dyes described in patent applications WO 95/115144, WO 95/01772 and EP 714 954, the content of which forms an integral part of the invention.
Among these compounds, mention may be made most particularly of the following dyes: 1,3-dimethyl-2-[[4-(dimethylamino)phenyl]azo]-1H-imidazolium chloride, 1,3-dimethyl-2-[(4-aminophenyl)azo]-1H-imidazolium chloride, 1-methyl-4-[(methylphenylhydrazono)methyl]pyridinium methyl sulphate.
Among the azo direct dyes that may also be mentioned are the following dyes described in the Colour Index International 3rd edition: Disperse Red 17, Acid Yellow 9, Acid Black 1, Basic Red 22, Basic Red 76, Basic Yellow 57, Basic Brown 16, Acid Yellow 36, Acid Orange 7, Acid Red 33, Acid Red 35, Basic Brown 17, Acid Yellow 23, Acid Orange 24, Disperse Black 9.
Mention may also be made of 1-(4′-amino-diphenylazo)-2-methyl-4-[bis(β-hydroxyethyl)-amino]benzene and 4-hydroxy-3-(2-methoxyphenylazo)-1-naphthalenesulphonic acid.
Among the quinone direct dyes that may be mentioned are the following dyes: Disperse Red 15, Solvent Violet 13, Acid Violet 43, Disperse Violet 1, Disperse Violet 4, Disperse Blue 1, Disperse Violet 8, Disperse Blue 3, Disperse Red 11, Acid Blue 62, Disperse Blue 7, Basic Blue 22, Disperse Violet 15, Basic Blue 99, and also the following compounds: 1-N-methylmorpholiniumpropylamino-4-hydroxyanthraquinone, 1-aminopropylamino-4-methylaminoanthraquinone, 1-amino-propylaminoanthraquinone, 5-β-hydroxyethyl-1,4-diaminoanthraquinone, 2-aminoethylaminoanthraquinone, 1,4-bis (β,γ-dihydroxypropylamino)anthraquinone.
Among the azine dyes that may be mentioned are the following compounds: Basic Blue 17, Basic Red 2.
Among the triarylmethane dyes that may be used according to the invention, mention may be made of the following compounds: Basic Green 1, Acid Blue 9, Basic Violet 3, Basic Violet 14, Basic Blue 7, Acid Violet 49, Basic Blue 26, Acid Blue 7.
Among the indoamine dyes that may be used according to the invention, mention may be made of the following compounds:
Among the natural direct dyes that may be used according to the invention, mention may be made of lawsone, juglone, alizarin, purpurin, carminic acid, kermesic acid, purpurogallin, protocatechaldehyde, indigo, isatin, curcumin, spinulosin and apigenidin. Extracts or decoctions containing these natural dyes may also be used, and especially henna-based poultices or extracts.
The amount of oxidation bases present in the dye composition obtained by the process of the present invention is generally between 0.001% and 10% by weight and preferably between 0.005% and 6% by weight approximately relative to the total weight of the dye composition.
The amount of couplers present in the dye composition obtained by the process of the present invention is generally between 0.001% and 10% by weight and preferably between 0.005% and 6% by weight approximately relative to the total weight of the dye composition.
The amount of direct dyes present in the dye composition obtained by the process of the present invention is generally between 0.001% and 20% by weight approximately and even more preferably between 0.005% and 10% by weight approximately relative to the total weight of the ready-to-use composition.
The oxidizing agents that are useful in the context of the present invention are the oxidizing agents conventionally used in the field of hair treatment. Such oxidizing agents are, for example, hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulphates, peracids and oxidase enzymes, among which mention may be made of peroxidases, 2-electron oxidoreductases such as uricases and 4-electron oxygenases, for instance laccases. Hydrogen peroxide is particularly preferred.
The cationic conditioners that are useful in the present invention are conditioners that are conventional in the field of hair treatment. Such agents are, for example, cationic monomers or cationic polymers.
The cationic conditioners of polymeric type that may be used in accordance with the present invention may be chosen from all those already known per se as improving the cosmetic properties of hair treated with detergent compositions, i.e. especially those described in patent application EP-A-0 337 354 and in French patent applications FR-A-2 270 846, 2 383 660, 2 598 611, 2 470 596 and 2 519 863.
Even more generally, for the purposes of the present invention; the term “cationic polymers” denotes any polymer comprising cationic groups and/or groups that may be ionized into cationic groups.
The cationic polymers that are preferred are chosen from those containing units comprising primary, secondary, tertiary and/or quaternary amine groups that either may form part of the main polymer chain or may be borne by a side substituent directly attached thereto.
The cationic polymers used generally have a number average molecular mass of between 500 and 5×106 approximately and preferably between 103 and 3×106 approximately.
Among the cationic polymers that may be mentioned more particularly are polymers of the polyamine, polyamino amide and polyquaternary ammonium type. These are known products.
The polymers of the polyamine, polyamino amide and polyquaternary ammonium type that pay be used in accordance with the present invention, and that may especially be mentioned, are those described in French patents Nos 2 505 348 and 2 542 997. Among these polymers, mention may be made of:
The copolymers of family (1) can also contain one or more units derived from comonomers which may be chosen from the family of acrylamides, methacrylamides, diacetone acrylamides, acrylamides and methacrylamides substituted on the nitrogen with lower (C1-C4) alkyls, acrylic or methacrylic acids or esters thereof, vinyllactams such as vinylpyrrolidone or vinylcaprolactam, and vinyl esters.
Thus, among these copolymers of family (1), mention may be made of:
The cellulose ether derivatives comprising quaternary ammonium groups, which are described in French patent 1 492 597 and in particular the polymers sold under the names “JR” (JR 400, JR 125, JR 30M) or “LR” (LR 400, LR 30M) by the company Amerchol. These polymers are also defined in the CTFA dictionary as hydroxyethylcellulose quaternary ammoniums that have reacted with an epoxide substituted with a trimethylammonium group.
The cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer are described especially in U.S. Pat. No. 4,131,576, such as hydroxyalkylcelluloses, for instance hydroxymethyl-, hydroxyethyl- or hydroxypropylcelluloses grafted especially with a methacryloylethyltrimethylammonium, methacrylamidopropyltrimethylammonium or dimethyl-diallylammonium salt.
The commercial products corresponding to this definition are more particularly the products sold under the names “Celquat® L 200” and “Celquat® H 100” by the company National Starch.
The cationic galactomannan gums are described more particularly in U.S. Pat. Nos. 3,589,578 and 4,031,307, in particular guar gums containing trialkyl-ammonium cationic groups. Use is made, for example, of guar gums modified with a salt (e.g. chloride) of 2,3-epoxypropyltrimethylammonium.
Such products are sold especially under the trade names Jaguar® C13 S, Jaguar® C 15, Jaguar® C 17 or Jaguar® C162 by the company Meyhall.
Among these derivatives, mention may be made more particularly of the adipic acid/dimethylamino-hydroxypropyl/diethylenetriamine polymers sold under the name “Cartaretine® F, F4 or F8” by the company Sandoz.
Polymers of this type are sold in particular under the name “Hercosett® 57” by the company Hercules Inc. or alternatively under the names “PD 170” or “Delsette® 101” by the company Hercules in the case of the adipic acid/epoxypropyl/diethylenetriamine copolymer.
R10 and R11, independently of each other, preferably denote an alkyl group containing from 1 to 4 carbon atoms.
Among the polymers defined above, mention may be made more particularly of the dimethyldiallyl-ammonium chloride homopolymer sold under the name “Merquat® 100” by the company Nalco (and its homologues of low weight-average molecular mass) and copolymers of diallyldimethylammonium chloride and of acrylamide, sold under the name “Merquat® 550”.
in which formula (XVIII):
R13, R14, R15 and R16, which may be identical or different, represent aliphatic, alicyclic or arylaliphatic radicals containing from 1 to 20 carbon atoms or lower hydroxyalkylaliphatic radicals, or alternatively R13, R14, R15 and R16, together or separately, constitute, with the nitrogen atoms to which they are attached, heterocycles optionally containing a second hetero atom other than nitrogen, or alternatively R13, R14, R15 and R16 represent a linear or branched C1-C6 alkyl radical substituted with a nitrile, ester, acyl or amide group or a group —CO—O—R17-D or —CO—NH—R17-D where R17 is an alkylene and D is a quaternary ammonium group;
A1 and B1 represent polymethylene groups containing from 2 to 20 carbon atoms, which groups may be linear or branched, saturated or unsaturated, and which may contain, linked to or intercalated in the main chain, one or more aromatic rings or one or more oxygen or sulphur atoms or sulphoxide, sulphone, disulphide, amino, alkylamino, hydroxyl, quaternary ammonium, ureido, amide or ester groups, and
X− denotes an anion derived from a mineral or organic acid;
A1, R13 and R15 can form, with the two nitrogen atoms to which they are attached, a piperazine ring; in addition, if A1 denotes a linear or branched, saturated or unsaturated alkylene or hydroxyalkylene radical, B1 can also denote a group (CH2)n—CO-D-OC—(CH2)n—
in which D denotes:
a) a glycol residue of formula: —O-Z-O—, where Z denotes a linear or branched hydrocarbon-based radical or a group corresponding to one of the following formulae:
where x and y denote an integer from 1 to 4, representing a defined and unique degree of polymerization or any number from 1 to 4 representing an average degree of polymerization;
b) a bis-secondary diamine residue such as a piperazine derivative;
c) a bis-primary diamine residue of formula: —NH—Y—NH—, where Y denotes a linear or branched hydrocarbon-based radical, or alternatively the divalent radical
d) a ureylene group of formula: —NH—CO—NH—.
Preferably, X− is an anion such as chloride or bromide.
These polymers generally have a number-average molecular mass of between 1000 and 100 000.
Polymers of this type are described in particular in French patents 2 320 330, 2 270 846, 2 316 271, 2 336 434 and 2 413 907 and U.S. Pat. Nos. 2,273,780, 2,375,853, 2,388,614, 2,454,547, 3,206,462, 2,261,002, 2,271,378, 3,874,870, 4,001,432, 3,929,990, 3,966,904, 4,005,193, 4,025,617, 4,025,627, 4,025,653, 4,026,945 and 4,027,020.
It is more particularly possible to use polymers that consist of repeating units corresponding to the formula:
in which R1, R2, R3 and R4, which may be identical or different, denote an alkyl or hydroxyalkyl radical containing from 1 to 4 carbon atoms approximately, n and p are integers ranging from 2 to 20 approximately, and X− is an anion derived from a mineral or organic acid.
One compound of formula (XIX) which is particularly preferred is the one for which R1, R2, R3 and R4 represent a methyl radical and n=3, p=6 and X=Cl, which is known as Hexadimethrine chloride according to the INCI (CTFA) nomenclature.
(9) polyquaternary ammonium polymers consisting of units of formula (XX):
in which formula:
R18, R19, R20 and R21, which may be identical or different, represent a hydrogen atom or a methyl, ethyl, propyl, β-hydroxyethyl, β-hydroxypropyl or —CH2CH2(OCH2CH2)pOH radical,
where p is equal to 0 or to an integer between 1 and 6, with the proviso that R18, R19, R20 and R21 do not simultaneously represent a hydrogen atom,
r and s, which may be identical or different, are integers between 1 and 6,
q is equal to 0 or to an integer between 1 and 34,
X− denotes an anion such as a halide,
A denotes a dihalide radical or preferably represents —CH2—CH2—O—CH2—CH2—.
Such compounds are described in particular in patent application EP-A-122 324.
Among these compounds, mention may be made, for example, of the products “Mirapol® A 15”, “Mirapol® AD1”, “Mirapol® AZ1” and “Mirapol® 175” sold by the company Miranol.
Other cationic polymers that can be used in the context of the invention are cationic proteins or cationic protein hydrolysates, polyalkyleneimines, in particular polyethyleneimines, polymers containing vinylpyridine or vinylpyridinium units, condensates of polyamines and of epichlorohydrin, quaternary polyureylenes and chitin derivatives.
Among all the cationic polymers that may be used in the context of the present invention, it is preferred to use quaternary cellulose ether derivatives such as the products sold under the name “JR 400” by the company Amerchol, cationic cyclopolymers, in particular the dimethyldiallylammonium chloride homopolymers or copolymers sold under the names “Merquat® 1000”, “Merquat® 550” and “Merquat® S” by the company Nalco, quaternary polymers of vinylpyrrolidone and of vinylimidazole, and mixtures thereof.
The cationic proteins or protein hydrolysates are, in particular, chemically modified polypeptides bearing quaternary ammonium groups at the end of the chain or grafted thereto. Their molecular mass can range, for example, from 1500 to 10 000 and in particular from 2000 to 5000 approximately. Among these compounds, mention may be made in particular of:
Among these protein hydrolysates, mention may be made of, inter alia:
These various products are sold by the company Croda.
Other quaternized proteins or hydrolysates are, for example, those corresponding to the formula:
in which X− is an anion of an organic or mineral acid, A denotes a protein residue derived from hydrolysates of a protein, especially of collagen, R5 denotes a lipophilic group containing up to 30 carbon atoms and R6 represents an alkylene group having 1 to 6 carbon atoms. Mention may be made, for example, of the products sold by the company Inolex under the name “Lexein® QX 3000”, referred to in the CTFA dictionary as “Cocotrimonium Collagen Hydrolysate”.
Mention may also be made of quaternized plant proteins such as wheat, corn or soybean proteins: as quaternized wheat proteins, mention may be made of those sold by the company Croda under the names “Hydrotriticum WQ or QM”, referred to in the CTFA dictionary as “Cocodimonium Hydrolysed Wheat Protein”, “Hydrotriticum QL”, referred to in the CTFA dictionary as “Laurdimonium Hydrolysed Wheat Protein” or “Hydrotriticum QS”, referred to in the CTFA dictionary as “Steardimonium Hydrolysed Wheat Protein”.
The cationic surfactants are especially chosen from quaternary ammonium salts, quaternary ammonium salts of imidazoline, diquaternary ammonium salts, and quaternary ammonium salts containing at least one ester function.
The cationic surfactants may be chosen from:
The cationic surfactant is preferably a behenyltrimethylammonium salt (for example chloride).
R3 and R4 are chosen in particular from (C12-C22)alkylamido(C2-C6)alkyl and (C12-C22)alkylacetate radicals.
The cationic surfactant is preferably a stearamidopropyldimethyl(myristyl acetate)ammonium salt (for example chloride);
Use is made more particularly of the ammonium salts of formula (XXV) in which:
Such compounds are sold, for example, under the names Dehyguart® by the company Cognis, Stepanquat® by the company Stepan, Noxamium® by the company Ceca, and Rewoquat® WE 18 by the company Rewo-Witco.
Among the quaternary ammonium salts that are preferred are stearamidopropyldimethyl(myristyl acetate)ammonium chloride, sold under the name “Ceraphyl® 70” by the company Van Dyk, and Quaternium-27 or Quaternium-83 sold by the company Witco.
The concentration of active agents in the compositions that are useful in the process of the present invention is between 0.001% and 20% and preferably between 0.01% and 10% relative to the total weight of the composition.
The heating iron that is useful in the context of the invention is a heating iron conventionally used in the hair field. Such an iron, for example a curling iron or a smoothing iron, is well known in the field of hair treatment. For example, irons that are useful for performing the present invention are flat or round irons described in U.S. Pat. Nos. 4,103,145, 4,308,878, 5,983,903, 5,957,140 and 5,494,058.
In the context of the invention, the temperature is greater than 60° C. Preferably, this temperature is between 60° C. and 220° C. Even more preferably, this temperature is between 120 and 200° C.
The iron may be applied to the hair by successive touches or by sliding it along the hair.
It is possible, between the application of the hair composition and the application of the heating iron to the keratin fibres, to include a rest phase. It is also possible to include a rinsing step before applying the iron to the fibres.
The hair composition according to the present invention contains active agents of the type described above, in a medium that is suitable for treating the hair. Such a medium generally consists of water or a mixture of water and at least one organic solvent to dissolve the compounds which would not be sufficiently soluble in water. As organic solvent, mention maybe made, for example, of C1-C4 lower alkanols, such as ethanol and isopropanol; polyols and polyol ethers such as 2-butoxyethanol, propylene glycol, propylene glycol monomethyl ether, diethylene glycol monoethyl ether and monomethyl ether, as well as aromatic alcohols such as benzyl alcohol or phenoxyethanol, and mixtures thereof.
The solvents are preferably present in proportions preferably of between 1% and 40% by weight approximately relative to the total weight of the dye composition, and even more preferably between 5% and 30% by weight approximately.
The composition may also contain various adjuvants conventionally used in compositions for dyeing the hair, such as anionic, cationic, nonionic, amphoteric or zwitterionic surfactants or mixtures thereof, anionic, cationic, nonionic, amphoteric or zwitterionic polymers or mixtures thereof, mineral or organic thickeners, and in particular anionic, cationic, nonionic and amphoteric associative polymeric thickeners, antioxidants, penetration agents, sequestering agents, fragrances, buffers, dispersing agents, packaging agents such as, for example, silicones, which may or may not be volatile or modified, film-forming agents, ceramides, preserving agents and opacifiers.
Preferably, the compositions used according to the invention contain a thickening polymer. According to one particularly preferred embodiment, the thickening polymer is a superabsorbent polymer.
The above adjuvants are generally present in an amount for each of them of between 0.01% and 20% by weight relative to the weight of the composition.
Needless to say, a person skilled in the art will take care to select this or these optional additional compound(s) such that the advantageous properties intrinsically associated with the treatment composition in accordance with the invention are not, or are not substantially, adversely affected by the envisaged addition(s).
The pH of the composition is generally between about 3 and 12 and preferably between about 5 and 11. It may be adjusted to the desired value using acidifying or basifying agents usually used in the dyeing of keratin fibres, or alternatively using standard buffer systems.
Among the acidifying agents that may be mentioned, for example, are mineral or organic acids such as hydrochloric acid, orthophosphoric acid, sulphuric acid, carboxylic acids such as acetic acid, tartaric acid, citric acid and lactic acid, and sulphonic acids.
Among the basifying agents that may be mentioned, for example, are aqueous ammonia, alkaline carbonates, alkanolamines such as mono-, di- and triethanolamine and derivatives thereof, sodium hydroxide, potassium hydroxide and the compounds of formula (II) below.
in which W is a propylene residue which is unsubstituted or substituted with a hydroxyl group or a C1-C4 alkyl radical; Ra, Rb, Rc and Rd, which may be identical or different, represent a hydrogen atom, a C1-C4 alkyl radical or a C1-C4 hydroxyalkyl radical.
The composition applied to the keratin fibres may be in various forms, such as in the form of liquids, creams or gels or in any other form that is suitable for dyeing keratin fibres, and especially human hair.
A subject of the invention is also a composition containing at least one superabsorbent polymer and at least one active agent chosen from hair dyes, oxidizing agents and cationic conditioners. According to one particular embodiment, the composition for dyeing keratin fibres comprises, in a medium that is suitable for dyeing keratin fibres, at least one superabsorbent polymer and at least one hair dye, and optionally an oxidizing agent or a cationic conditioner, the dye, the oxidizing agent or the conditioner being as defined above.
For the purposes of the present invention, the term “superabsorbent polymer” means any polymer having a free swelling capacity of greater than 20 and preferably greater than 30, at room temperature (25° C.) and at atmospheric pressure.
This value, which is equivalent to the amount of fluid absorbed per gram of polymer, is determined by dispersing 0.5 g of polymer in 150 g of 1% sodium chloride solution, waiting 20 minutes, filtering the solution not absorbed through a 150 μm filter for 20 minutes and weighing the water not absorbed.
Examples of superabsorbent polymers that may be mentioned include those described in U.S. Pat. Nos. 3,926,891, 4,190,562, 4,293,609, 4,424,247 and 4,535,098.
The superabsorbent polymers are preferably crosslinked polyacrylates.
Particular examples that may be mentioned are the products sold by the company Technical Absorbents under the reference Oasis Fibre 6 mm Superabsorbent Type 101.
Preferably, the concentration of superabsorbent polymer is between 0.05% and 20% and more preferably between 0.1% and 10% relative to the total weight of the composition.
The examples that follow illustrate the invention without, however, limiting the scope.
The following hair compositions are prepared:
Oasis Fibre 6 mm Superabsorbent Type 101
Basic Red 51 dye
qs 100 g
Oasis Fibre 6 mm Superabsorbent Type 101
Basic Red 51 dye
Shorea Robusta Seed Butter
6.9 × 10−3
Cyclopentasiloxane and Dimethiconol
6.9 × 10−3
Oasis Fibre 6 mm Superabsorbent Type 101
Basic Red 51 dye
Shorea Robusta Seed Butter
Cyclopentasiloxane and Dimethiconol
The compositions are applied to two pairs of permanent-waved (BP) and non-permanent-waved (BN) locks. One of the locks of each of the pairs is treated with a heating iron at a temperature of 180° C. by sliding it along the fibres.
After rinsing, washing with shampoo, rinsing and drying, each lock is evaluated before and after dyeing, in the L*a*b* system, using a Minolta® CM 2002 spectrophotometer (illuminant D65).
In the L*a*b* system, the three parameters denote, respectively, the lightness (L*), the hue (a*) and the saturation (b*). According to this system, the higher the value of L, the paler or weaker the colour. Conversely, the lower the value of L, the darker or stronger the colour. a* and b* indicate two colour axes; a* indicates the green/red colour axis and b* indicates the blue/yellow colour axis.
The locks treated with the iron are more strongly coloured than those not treated with the iron.
Colorimetric results of the locks
In all cases, the value L* with treatment with the iron is lower than that without treatment with the iron. The hues are thus stronger with the treatment according to the present invention.
It is also observed that the hues obtained are more chromatic with the treatment with the iron, the chromaticity being calculated by (a*2+b*2)1/2.
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|Citing Patent||Filing date||Publication date||Applicant||Title|
|US8691196 *||Jun 28, 2006||Apr 8, 2014||L'oreal||Photoprotective treatment of keratin fibers by application of heat|
|US20070056121 *||Jun 28, 2006||Mar 15, 2007||L'oreal||Photoprotective treatment of keratin fibers by application of heat|
|U.S. Classification||8/405, 8/558, 8/557, 8/407, 8/463, 8/552, 8/435, 8/406|
|International Classification||A45D1/00, A45D7/02, A61Q5/10, A61K8/81, A61K8/02, A61Q5/06|
|Cooperative Classification||A45D7/02, A61K8/027, A61K8/8152, A61K2800/54, A61Q5/065, A61Q5/10, A61K2800/42, A61K8/4946, A61K2800/24, A45D1/00, A61K8/02|
|European Classification||A45D7/02, A61K8/02N4, A61K8/81K4, A61K8/02, A61Q5/10, A61Q5/06D, A61K8/49F1|
|Jan 26, 2007||AS||Assignment|
Owner name: L'OREAL S.A., FRANCE
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:DE LA METTRIE, ROLAND;REEL/FRAME:018859/0563
Effective date: 20051128
|Mar 5, 2007||AS||Assignment|
Owner name: L'OREAL S.A., FRANCE
Free format text: CORRECTION TO THE SERIAL NUMBER ON REEL 018859, AND FRAME 0563;ASSIGNOR:DE LA METTRIE, ROLAND;REEL/FRAME:019018/0766
Effective date: 20051128
|Dec 22, 2009||CC||Certificate of correction|
|Mar 7, 2013||FPAY||Fee payment|
Year of fee payment: 4
|Jun 9, 2017||REMI||Maintenance fee reminder mailed|